The basis for limited specificity and MHC restriction in a T cell receptor interface

Kurt H. Piepenbrink, Sydney J. Blevins, Daniel R. Scott, Brian M. Baker

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

αβ T cell receptors (TCRs) recognize peptides presented by major histocompatibility complex (MHC) proteins using multiple complementarity-determining region (CDR) loops. TCRs display an array of poorly understood recognition properties, including specificity, crossreactivity and MHC restriction. Here we report a comprehensive thermodynamic deconstruction of the interaction between the A6 TCR and the Tax peptide presented by the class I MHC HLA-A∗0201, uncovering the physical basis for the receptor's recognition properties. Broadly, our findings are in conflict with widely held generalities regarding TCR recognition, such as the relative contributions of central and peripheral peptide residues and the roles of the hypervariable and germline CDR loops in engaging peptide and MHC. Instead, we find that the recognition properties of the receptor emerge from the need to engage the composite peptide/MHC surface, with the receptor utilizing its CDR loops in a cooperative fashion such that specificity, crossreactivity and MHC restriction are inextricably linked.

Original languageEnglish (US)
Article number1948
JournalNature communications
Volume4
DOIs
StatePublished - Jun 5 2013

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T-Cell Antigen Receptor
Complementarity Determining Regions
Major Histocompatibility Complex
constrictions
peptides
Peptides
Thermodynamics
cells
Composite materials
Proteins
proteins
thermodynamics
composite materials
interactions

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Chemistry(all)
  • Physics and Astronomy(all)
  • Medicine(all)

Cite this

The basis for limited specificity and MHC restriction in a T cell receptor interface. / Piepenbrink, Kurt H.; Blevins, Sydney J.; Scott, Daniel R.; Baker, Brian M.

In: Nature communications, Vol. 4, 1948, 05.06.2013.

Research output: Contribution to journalArticle

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